Disease #01698 (GDHS (ataxia, cerebellar, and hypogonadotropic hypogonadism), OMIM:212840)

Official abbreviation GDHS
Name ataxia, cerebellar, and hypogonadotropic hypogonadism
OMIM ID 212840
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene RNF216
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00409555 K6852 PubMed: Oishi 2018 - F - Japan - - - - - GDHS best corrected visual acuity: 0.07; electroretinogram , rod: n.a., cone: n.a. CYP4V2 CYP4V2 1 1 LOVD
00430226 patient - - M yes Turkey Turkey - - - - GDHS - RNF216 RNF216 1 1 Ebru Erzurumluoglu Gokalp
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